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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977584inversion1nstd209human GRCh38 chrX: 51,536,782-52,222,904 , GRCh37.p13 chrX|NW_004070877.1: 1,249,897-1,936,019 , GRCh37.p13 chrX: 51,279,634-51,966,031 MAGED1, GSPT2, 17 more genes
    nsv5877274copy number variation1nstd209human GRCh38 chrX: 48,251,965-52,619,725 , GRCh37.p13 chrX|NW_004070877.1: 1-2,332,840 PLP2, SSXP8, 146 more genes
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4757986inversion1nstd199human GRCh37 chrX: 51,784,616-51,955,702 , GRCh38.p12 chrX: 52,041,520-52,212,575 MAGED4B, LOC401589, 5 more genes
    nsv4730085inversion28nstd198human GRCh37.p13 chrX: 51,738,884-51,958,216 , GRCh38 chrX: 51,995,788-52,215,089 , GRCh37.p13 chrX|NW_004070877.1: 1,708,903-1,928,204 MAGED4B, LOC401589, 5 more genes
    nsv4728653copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,102,202-52,685,635 , GRCh38.p12 chrX: 48,242,767-52,656,585 CCNB3, AKAP4, 150 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4728228copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,178,413-52,686,510 , GRCh38.p12 chrX: 48,318,978-52,657,460 MRPL32P1, LOC100421603, 142 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4680157copy number variation1nstd189human GRCh37.p13 chrX: 48,059,259-52,748,576 , GRCh38.p12 chrX: 48,199,823-52,719,527 CACNA1F, CLCN5, 157 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4454441copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,224,266-52,744,574 , GRCh38.p12 chrX: 48,364,831-52,715,525 LOC105373205, RBM22P6, 143 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4450820copy number variation1nstd102humanPathogenic GRCh37 chrX: 40,572,613-92,796,528 , GRCh38.p12 chrX: 40,713,361-93,541,529 HNRNPA1P25, MPV17L2P1, 755 more genes
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